Clinical Trials Directory

Trials / Unknown

UnknownNCT05311696

Residential Retreat for Veterans and First-responders

Examining the Efficacy and Feasibility of a Residential Retreat Program for PTSD in First-responders and Veterans: A Non-randomized Controlled Study

Status
Unknown
Phase
Study type
Observational
Enrollment
70 (estimated)
Sponsor
Valhalla Project Niagara · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the potential efficacy and feasibility of a residential retreat program to address PTSD symptoms in Veterans and First-responders

Detailed description

After obtaining written consent, participants will complete their program as they had previously intended. Each wave of the residential retreat program will last 5 days. During the program, participants will complete the study questionnaires. They will complete these questionnaires again 1 month after the completion of the program. As a control, individuals completing the program in the online format will also be asked to provide written consent and will complete the questionnaires during the program and 1-month after its completion.

Conditions

Interventions

TypeNameDescription
OTHERpsychoeducationThe program consists of psychoeducational material regarding PTSD, demonstration of various stress management techniques, and social cohesion activities

Timeline

Start date
2022-03-27
Primary completion
2022-11-21
Completion
2023-11-21
First posted
2022-04-05
Last updated
2022-04-05

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05311696. Inclusion in this directory is not an endorsement.